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PubMed:21903317 JSONTXT 51 Projects

Annnotations TAB TSV DIC JSON TextAE Lectin_function IAV-Glycan

Id Subject Object Predicate Lexical cue
T1 53-58 GeneOrGeneProduct denotes renin
T2 77-83 DiseaseOrPhenotypicFeature denotes anemia
T3 85-98 DiseaseOrPhenotypicFeature denotes hyperuricemia
T4 104-107 DiseaseOrPhenotypicFeature denotes CKD
T5 158-163 GeneOrGeneProduct denotes renin
T6 165-168 GeneOrGeneProduct denotes REN
T7 176-200 DiseaseOrPhenotypicFeature denotes renal tubular dysgenesis
T8 228-233 DiseaseOrPhenotypicFeature denotes death
T9 250-264 DiseaseOrPhenotypicFeature denotes kidney failure
T10 269-289 DiseaseOrPhenotypicFeature denotes pulmonary hypoplasia
T11 319-328 DiseaseOrPhenotypicFeature denotes fetopathy
T12 339-378 ChemicalEntity denotes angiotensin-converting enzyme inhibitor
T13 382-410 ChemicalEntity denotes angiotensin receptor blocker
T14 459-462 GeneOrGeneProduct denotes REN
T15 509-522 DiseaseOrPhenotypicFeature denotes hyperuricemia
T16 524-530 DiseaseOrPhenotypicFeature denotes anemia
T17 536-558 DiseaseOrPhenotypicFeature denotes chronic kidney disease
T18 560-563 DiseaseOrPhenotypicFeature denotes CKD
T19 605-608 GeneOrGeneProduct denotes REN
T20 675-678 GeneOrGeneProduct denotes REN
T21 704-717 DiseaseOrPhenotypicFeature denotes hyperuricemia
T22 722-725 DiseaseOrPhenotypicFeature denotes CKD
T23 778-782 GeneOrGeneProduct denotes UMOD
T24 784-794 GeneOrGeneProduct denotes uromodulin
T25 800-805 GeneOrGeneProduct denotes HNF1B
T26 807-835 GeneOrGeneProduct denotes hepatocyte nuclear factor 1β
T27 883-928 SequenceVariant denotes thymidine to cytosine mutation at position 28
T28 936-939 GeneOrGeneProduct denotes REN
T29 978-1030 SequenceVariant denotes tryptophan to arginine substitution at amino acid 10
T30 1075-1082 SequenceVariant denotes c.28T>C
T31 1084-1090 SequenceVariant denotes p.W10R
T32 1125-1128 GeneOrGeneProduct denotes REN
T33 1158-1166 OrganismTaxon denotes patients
T34 1172-1175 DiseaseOrPhenotypicFeature denotes CKD
T35 1268-1271 GeneOrGeneProduct denotes REN
T36 1319-1325 DiseaseOrPhenotypicFeature denotes anemia
T37 1327-1340 DiseaseOrPhenotypicFeature denotes hyperuricemia
T38 1346-1349 DiseaseOrPhenotypicFeature denotes CKD
T39 1351-1357 DiseaseOrPhenotypicFeature denotes Anemia
T40 1458-1461 GeneOrGeneProduct denotes REN
T41 1552-1555 GeneOrGeneProduct denotes REN
T42 1565-1573 OrganismTaxon denotes patients
T43 1579-1582 DiseaseOrPhenotypicFeature denotes CKD
T44 1588-1601 DiseaseOrPhenotypicFeature denotes hyperuricemia
T45 1606-1612 DiseaseOrPhenotypicFeature denotes anemia